Variant #0000128808 (NC_000016.9:g.1840927G>A, NM_004970.2:c.1492C>T (IGFALS))
| Chromosome |
16 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1840927G>A |
| DNA change (hg38) |
g.1790926G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
IGFALS_000017 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs9282730 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0-0.02 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00035 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2008-09-12 18:44:29 +02:00 (CEST) |
| Date last edited |
2008-09-12 18:45:51 +02:00 (CEST) |

Variant on transcripts
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